Senior Clinical Research Associate (Bilingual) - Oncology - Canada (Remote)

Worldwide Clinical Trials; Quebec; Hybrid; CAD 70,000 - 100,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate in Canada to contribute across Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. The role involves managing research activities at sites, coordinating start-up activities, site training, and study maintenance while ensuring regulatory compliance and safety reporting.

Travel regionally is required, and fluency in English and French is expected.

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree OR Nursing Degree.
• Experience in Oncology is required.
• Fluent in written and verbal English and French is required.
• Candidates must reside in Canada.
• Willingness to travel regionally required.

Responsibilities

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects.
• Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded.
• Conduct study initiation visits (SIVs).
• While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements

Skills

English proficiency

Communication skills

Organizational skills

Independence

MS Office

CTMS

EDC Systems

Education

Bachelor's degree or Nursing degree

Tools

Microsoft Office

CTMS

EDC Systems

Job description

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) you will work alongside brilliant minds across therapeutic areas including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.

What You Will Do

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
• Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
• Conduct study initiation visits (SIVs)
• While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements

What You Will Bring To The Role

• Excellent interpersonal, oral, and written communication skills in English
• Superior organizational skills with attention to detail
• Ability to work with little or no supervision
• Proficiency in Microsoft Office, CTMS, and EDC Systems

Your Experience

• 5+ years of experience as a Clinical Research Associate
• 4-year university degree OR Nursing Degree
• Experience in Oncology is required
• Fluent in written and verbal English and French is required
• Candidates must reside in Canada
• Willingness to travel regionally required

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.